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Hesperadin

CAS No.
422513-13-1
Chemical Name:
Hesperadin
Synonyms
CS-408;Hesperadin;Hesperadine;Hesperadin, >=98%;Hesperadin USP/EP/BP;Hesperadin hydrochloride;Hesperadin (This product is unavailable in the U.S.);Hesperadin Hesperadine;(Z)-N-(2-Oxo-3-(phenyl((4-(piperidin-1-ylmethyl)phenyl)amino)methylene)indolin-5-yl)ethanesulf;(Z)-N-(2-oxo-3-(phenyl(4-(piperidin-1-ylmethyl)phenylamino)methylene)indolin-5-yl)ethanesulfonamide
CBNumber:
CB12537545
Molecular Formula:
C29H32N4O3S
Molecular Weight:
516.65
MDL Number:
MFCD18074526
MOL File:
422513-13-1.mol
Last updated:2023-05-18 11:31:10

Hesperadin Properties

Melting point 228 °C
Density 1.326
storage temp. Refrigerator
solubility DMSO, Methanol
form Solid
pka 9.14±0.20(Predicted)
color Yellow
CAS DataBase Reference 422513-13-1
FDA UNII PTR491OS14

Hesperadin price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 375680 Hesperadin - CAS 422513-13-1 - Calbiochem Hesperadin primarily used in Inhibition. 422513-13-1 5mg $280 2024-03-01 Buy
Cayman Chemical 24199 Hesperadin ≥98% 422513-13-1 1mg $49 2024-03-01 Buy
Cayman Chemical 24199 Hesperadin ≥98% 422513-13-1 5mg $202 2024-03-01 Buy
Cayman Chemical 24199 Hesperadin ≥98% 422513-13-1 10mg $310 2024-03-01 Buy
Cayman Chemical 24199 Hesperadin ≥98% 422513-13-1 25mg $711 2024-03-01 Buy
Product number Packaging Price Buy
375680 5mg $280 Buy
24199 1mg $49 Buy
24199 5mg $202 Buy
24199 10mg $310 Buy
24199 25mg $711 Buy

Hesperadin Chemical Properties,Uses,Production

Description

Hesperadin is a multi-kinase inhibitor. It inhibits human Aurora kinase B (IC50 = 250 nM) and its T. brucei homolog Aurora kinase-1 (IC50 = 40 nM) in in vitro kinase assays. Hesperadin (1 μM) inhibits AMPK, LCK, MKK1, MAPKAP-K1, CHK1, and PHK in a panel of 25 kinases. It also inhibits MEKK2 in ATPase and transphosphorylation assays with IC50s of 60 and 34 nM, respectively. Hesperadin (50-100 nM) induces polyploidy and defects in cytokinesis and spindle assembly as well as inhibits proliferation of HeLa cells and overrides mitotic arrest induced by paclitaxel or monastrol . Hesperadin also induces toxicity in HepG2 cells with a toxic concentration (TC50) value of less than 0.2 μM. It inhibits replication of clinical isolates of influenza A and B viruses with EC50s ranging from 0.22 to 2.21 μM in a plaque formation assay. Hesperadin inhibits the growth of T. brucei, L. major promastigotes and amastigotes, and P. falciparum with EC50 values ranging from 0.01 to 2.37 μM, but has less activity against T. cruzi (EC50 = 39 μM).

Uses

Hesperadin phosphorylates human mitotic protein complexes that control physiological changes within the cell to allow for proper and successful chromosome segregation. It also targets aurora kinases in cancer treatment, affecting the chromosomes’ regulation during mitosis.

Definition

ChEBI: An oxindole that is indolin-2-one which is substituted at position 5 by an (ethylsulfonyl)nitrilo group and at position 2 by a methylidene group, which is itself substituted by a phenyl group and a [4-(piperidin-1-ylmethyl)phenyl]amino group. An Aurora B k nase inhibitor, it is used to inhibit chromosome alignment and segregation.

References

[1]jetton n1, rothberg kg, hubbard jg, wise j, li y, ball hl, ruben l. the cell cycle as a therapeutic target against trypanosoma brucei: hesperadin inhibits aurora kinase-1 and blocks mitotic progression in bloodstream forms. mol microbiol. 2009 apr;72(2):442-58. doi: 10.1111/j.1365-2958.2009.06657.x. epub 2009 mar 6.
[2]hauf s1, cole rw, laterra s, zimmer c, schnapp g, walter r, heckel a, van meel j, rieder cl, peters jm. the small molecule hesperadin reveals a role for aurora b in correcting kinetochore-microtubule attachment and in maintaining the spindle assembly checkpoint. j cell biol. 2003 apr 28;161(2):281-94. epub 2003 apr 21.

Hesperadin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 110)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
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Biochempartner
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Hubei xin bonus chemical co. LTD
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career henan chemical co
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Dideu Industries Group Limited
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Zhejiang J&C Biological Technology Co.,Limited
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InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6391 58
LEAP CHEM CO., LTD.
+86-852-30606658 market18@leapchem.com China 24727 58
TargetMol Chemicals Inc.
support@targetmol.com United States 38463 58
ShenZhen Trendseen Biological Technology Co.,Ltd.
13417589054 trendseenbio@gmail.com China 11681 58

View Lastest Price from Hesperadin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Hesperadin pictures 2020-01-13 Hesperadin
422513-13-1
US $1.00 / g 1g 99% 1ton Career Henan Chemical Co
  • Hesperadin pictures
  • Hesperadin
    422513-13-1
  • US $1.00 / g
  • 99%
  • Career Henan Chemical Co

Hesperadin Spectrum

(Z)-N-(2-oxo-3-(phenyl(4-(piperidin-1-ylmethyl)phenylamino)methylene)indolin-5-yl)ethanesulfonamide Hesperadin Hesperadine N-[2,3-Dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]ethanesulfonamide Hesperadin Hesperadin, >=98% Hesperadin Hesperadin hydrochloride N-[(3Z)-2-Oxo-3-[phenyl-[4-(piperidin-1-ylMethyl)anilino]Methylidene]-1H-indol-5-yl]ethanesulfonaMide Hesperadine N-[2,3-Dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]ethanesulfonamide (Z)-N-(2-Oxo-3-(phenyl((4-(piperidin-1-ylmethyl)phenyl)amino)methylene)indolin-5-yl)ethanesulf N-[(3Z)-2-Oxo-3-(phenyl{[4-(1-piperidinylmethyl)phenyl]amino}methylen)-2,3-dihydro-1H-indol-5-yl]ethansulfonamid Hesperadin (This product is unavailable in the U.S.) CS-408 N-[2,3-Dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]-ethanesulfonamide hydrochloride Ethanesulfonamide, N-[2,3-dihydro-2-oxo-3-[(3Z)-phenyl[[4-(1-piperidinylmethyl)phenyl]amino]methylene]-1H-indol-5-yl]- Hesperadin USP/EP/BP 422513-13-1 Inhibitor Inhibitors